Evidence map›Paper›PMID 42159886›Full record

ReviewCurrent oncology reports2026

Sarcomas in Adolescents and Young Adults.

Jacob R Greenmyer, Wendy Allen-Rhoades

Abstract readReview
In one paragraph

Review in Current oncology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Jacob R GreenmyerPediatric Hematology and Oncology, Mayo Clinic, 200 First St. SW, Rochester, MN, 55905, USA.
Wendy Allen-RhoadesPediatric Hematology and Oncology, Mayo Clinic, 200 First St. SW, Rochester, MN, 55905, USA. allen-rhoades.wendy@mayo.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThis review aims to assess the current state of bone and soft tissue sarcomas (STS) management in the adolescent and young adult population (AYA) with a focus on Ewing sarcoma (EWS), osteosarcoma (OS), rhabdomyosarcoma (RMS), and non-rhabdomyosarcoma soft tissue sarcoma (NRSTS). RECENT

findingsThere has been a significant growth in novel agents available for bone sarcomas in the AYA population; trials continue to study the efficacy of these agents. The future of STS will likely include more single histology and targeted biologic studies. Joint pediatric and adult sarcoma clinical trials are feasible. AYAs continue to represent an underserved patient population in medical oncology. Collaboration between pediatric and adult practices may increase patient enrollment and enable single histology and biology specific studies. Trials for EWS, OS, RMS, and NRSTS should include both pediatric and adult patients whenever possible.

Indexed as

Bone NeoplasmsSarcomaAdolescentAdultHumansOsteosarcomaRhabdomyosarcomaSarcoma, EwingYoung AdultAdolescent and young adult (AYA)Ewing sarcomaNon-rhabdomyosarcoma soft tissue sarcoma (NRSTS)OsteosarcomaRhabdomyosarcomaSarcoma

Identifiers

PMID42159886
PMCPMC13190490

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.